Canonical Allele Identifier: CA2123456146

Gene: MYH7

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.23433738T= , CM000676.2:g.23433738T=	GRCh38
NC_000014.8:g.23902947T= , CM000676.1:g.23902947T=	GRCh37
NC_000014.7:g.22972787T=	NCBI36
NG_007884.1:g.6924A= , LRG_384:g.6924A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355349.4:c.-6A= MANE Select	ENSP00000347507.3:n.-6A=
ENST00000355349.3:c.-6A=	ENSP00000347507.3:n.-6A=
NM_000257.3:c.-6A=	NP_000248.2:n.-6A=
XR_245686.3:n.101A=
XM_017021340.1:c.-6A=	XP_016876829.1:n.-6A=
NM_000257.4:c.-6A= MANE Select	NP_000248.2:n.-6A=